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Brigatinib versus other second-generation ALK inhibitors as initial treatment of anaplastic lymphoma kinase positive non-small cell lung cancer with deep phenotyping: study protocol of the ABP trial
by
Stenzinger, Albrecht
, Christopoulos, Petros
, Krisam, Johannes
, Eickhoff, Regina
, Thomas, Michael
, Schneider, Marc A.
, Chung, Inn
, Bozorgmehr, Farastuk
, Mueller, Daniel W.
, Brückner, Lena
in
ALK+ NSCLC
/ Anaplastic lymphoma kinase
/ Anaplastic Lymphoma Kinase - drug effects
/ Biomedical and Life Sciences
/ Biomedicine
/ Brain cancer
/ Brigatinib
/ Cancer Research
/ Cancer therapies
/ Carcinoma, Non-Small-Cell Lung - drug therapy
/ Carcinoma, Non-Small-Cell Lung - pathology
/ Chemotherapy
/ Clinical Trials, Phase II as Topic
/ Disease progression
/ Drug resistance
/ Drug therapy
/ Health Promotion and Disease Prevention
/ Humans
/ Inhibitor drugs
/ Lung cancer
/ Lung cancer, Non-small cell
/ Lung Neoplasms - drug therapy
/ Lung Neoplasms - pathology
/ Lymphoma
/ Medical and radiation oncology
/ Medicine/Public Health
/ Metastases
/ Metastasis
/ Multicenter Studies as Topic
/ Mutation
/ Next-generation sequencing
/ Non-small cell lung cancer
/ Non-small cell lung carcinoma
/ Oncology
/ Organophosphorus Compounds - pharmacology
/ Organophosphorus Compounds - therapeutic use
/ Patient safety
/ Patients
/ Phenotype
/ Phenotyping
/ Prospective Studies
/ Protein Kinase Inhibitors - pharmacology
/ Protein Kinase Inhibitors - therapeutic use
/ Protein-tyrosine kinase
/ Pyrimidines - pharmacology
/ Pyrimidines - therapeutic use
/ Questionnaires
/ Resistance mutations
/ Small cell lung carcinoma
/ Study Protocol
/ Surgical Oncology
/ Thoracic surgery
/ Tumors
/ Tyrosine kinase inhibitors (TKI)
2021
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Brigatinib versus other second-generation ALK inhibitors as initial treatment of anaplastic lymphoma kinase positive non-small cell lung cancer with deep phenotyping: study protocol of the ABP trial
by
Stenzinger, Albrecht
, Christopoulos, Petros
, Krisam, Johannes
, Eickhoff, Regina
, Thomas, Michael
, Schneider, Marc A.
, Chung, Inn
, Bozorgmehr, Farastuk
, Mueller, Daniel W.
, Brückner, Lena
in
ALK+ NSCLC
/ Anaplastic lymphoma kinase
/ Anaplastic Lymphoma Kinase - drug effects
/ Biomedical and Life Sciences
/ Biomedicine
/ Brain cancer
/ Brigatinib
/ Cancer Research
/ Cancer therapies
/ Carcinoma, Non-Small-Cell Lung - drug therapy
/ Carcinoma, Non-Small-Cell Lung - pathology
/ Chemotherapy
/ Clinical Trials, Phase II as Topic
/ Disease progression
/ Drug resistance
/ Drug therapy
/ Health Promotion and Disease Prevention
/ Humans
/ Inhibitor drugs
/ Lung cancer
/ Lung cancer, Non-small cell
/ Lung Neoplasms - drug therapy
/ Lung Neoplasms - pathology
/ Lymphoma
/ Medical and radiation oncology
/ Medicine/Public Health
/ Metastases
/ Metastasis
/ Multicenter Studies as Topic
/ Mutation
/ Next-generation sequencing
/ Non-small cell lung cancer
/ Non-small cell lung carcinoma
/ Oncology
/ Organophosphorus Compounds - pharmacology
/ Organophosphorus Compounds - therapeutic use
/ Patient safety
/ Patients
/ Phenotype
/ Phenotyping
/ Prospective Studies
/ Protein Kinase Inhibitors - pharmacology
/ Protein Kinase Inhibitors - therapeutic use
/ Protein-tyrosine kinase
/ Pyrimidines - pharmacology
/ Pyrimidines - therapeutic use
/ Questionnaires
/ Resistance mutations
/ Small cell lung carcinoma
/ Study Protocol
/ Surgical Oncology
/ Thoracic surgery
/ Tumors
/ Tyrosine kinase inhibitors (TKI)
2021
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Brigatinib versus other second-generation ALK inhibitors as initial treatment of anaplastic lymphoma kinase positive non-small cell lung cancer with deep phenotyping: study protocol of the ABP trial
by
Stenzinger, Albrecht
, Christopoulos, Petros
, Krisam, Johannes
, Eickhoff, Regina
, Thomas, Michael
, Schneider, Marc A.
, Chung, Inn
, Bozorgmehr, Farastuk
, Mueller, Daniel W.
, Brückner, Lena
in
ALK+ NSCLC
/ Anaplastic lymphoma kinase
/ Anaplastic Lymphoma Kinase - drug effects
/ Biomedical and Life Sciences
/ Biomedicine
/ Brain cancer
/ Brigatinib
/ Cancer Research
/ Cancer therapies
/ Carcinoma, Non-Small-Cell Lung - drug therapy
/ Carcinoma, Non-Small-Cell Lung - pathology
/ Chemotherapy
/ Clinical Trials, Phase II as Topic
/ Disease progression
/ Drug resistance
/ Drug therapy
/ Health Promotion and Disease Prevention
/ Humans
/ Inhibitor drugs
/ Lung cancer
/ Lung cancer, Non-small cell
/ Lung Neoplasms - drug therapy
/ Lung Neoplasms - pathology
/ Lymphoma
/ Medical and radiation oncology
/ Medicine/Public Health
/ Metastases
/ Metastasis
/ Multicenter Studies as Topic
/ Mutation
/ Next-generation sequencing
/ Non-small cell lung cancer
/ Non-small cell lung carcinoma
/ Oncology
/ Organophosphorus Compounds - pharmacology
/ Organophosphorus Compounds - therapeutic use
/ Patient safety
/ Patients
/ Phenotype
/ Phenotyping
/ Prospective Studies
/ Protein Kinase Inhibitors - pharmacology
/ Protein Kinase Inhibitors - therapeutic use
/ Protein-tyrosine kinase
/ Pyrimidines - pharmacology
/ Pyrimidines - therapeutic use
/ Questionnaires
/ Resistance mutations
/ Small cell lung carcinoma
/ Study Protocol
/ Surgical Oncology
/ Thoracic surgery
/ Tumors
/ Tyrosine kinase inhibitors (TKI)
2021
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Brigatinib versus other second-generation ALK inhibitors as initial treatment of anaplastic lymphoma kinase positive non-small cell lung cancer with deep phenotyping: study protocol of the ABP trial
Journal Article
Brigatinib versus other second-generation ALK inhibitors as initial treatment of anaplastic lymphoma kinase positive non-small cell lung cancer with deep phenotyping: study protocol of the ABP trial
2021
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Overview
Background
Availability of potent anaplastic lymphoma kinase (ALK) tyrosine kinase inhibitors (TKI) has pushed the median survival of ALK
+
non-smallcell lung cancer (NSCLC) patients to over five years. In particular, second-generation ALK TKI have demonstrated superiority compared to the first-generation compound crizotinib and are meanwhile standard first-line treatment. However, clinical courses of individual patients vary widely, with secondary development of drug resistance and intracranial progression remaining important problems. While these limitations highlight the need for better disease monitoring and additional therapeutic tools, molecular tumor features are increasingly recognized as crucial determinants of clinical outcome. This trial aims to optimize management of ALK
+
NSCLC by analyzing the efficacy of second-generation ALK inhibitors in conjunction with deep longitudinal phenotyping across two treatment lines.
Methods/design
In this exploratory prospective phase II clinical trial, newly diagnosed ALK
+
NSCLC patients will be randomized into two treatment arms, stratified by presence of brain metastases and ECOG performance status: brigatinib (experimental arm) vs. any other approved second-generation ALK TKI. Tumor tissue and blood samples will be collected for biomarker analysis at the beginning and throughout the study period to investigate baseline molecular tumor properties and analyze the development of acquired drug resistance. In addition, participating investigators and patients will have the possibility of fast-track molecular tumor and ctDNA profiling at the time of disease progression using state-of-the-art next-generation sequencing (NGS), in order to support decisions regarding next-line therapy.
Discussion
Besides supporting therapeutic decisions for enrolled patients, the ABP trial primarily aims to deepen the understanding of the underlying biology and facilitate development of a framework for individualized management of ALK
+
NSCLC according to molecular features. Patients with low molecular risk and the perspective of a “chronic disease” will be distinguished from “high-risk” cases, molecular properties of which will be utilized to elaborate improved methods of non-invasive monitoring and novel preclinical models in order to advance therapeutic strategies.
Trial registration
Clinicaltrials.gov
, NCT04318938. Registered March 182,020,
https://www.clinicaltrials.gov/ct2/show/NCT04318938
Eudra-CT, 2019–001828-36. Registered September 302,019,
https://www.clinicaltrialsregister.eu/ctr-search/search?query=2019-001828-36
Publisher
BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
Subject
/ Anaplastic Lymphoma Kinase - drug effects
/ Biomedical and Life Sciences
/ Carcinoma, Non-Small-Cell Lung - drug therapy
/ Carcinoma, Non-Small-Cell Lung - pathology
/ Clinical Trials, Phase II as Topic
/ Health Promotion and Disease Prevention
/ Humans
/ Lung Neoplasms - drug therapy
/ Lymphoma
/ Medical and radiation oncology
/ Multicenter Studies as Topic
/ Mutation
/ Non-small cell lung carcinoma
/ Oncology
/ Organophosphorus Compounds - pharmacology
/ Organophosphorus Compounds - therapeutic use
/ Patients
/ Protein Kinase Inhibitors - pharmacology
/ Protein Kinase Inhibitors - therapeutic use
/ Pyrimidines - therapeutic use
/ Tumors
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